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MeSH keywords -> Related genes, diseases (OMIM)


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01 Amelogenesis Imperfecta [NCBI]

Gene


 Gene Link Information
Gain		 01
LOC619531 [NCBI] 0.000438875
AIH3 [NCBI] 0.000438875
AMELX [NCBI] 0.00029445
ENAM [NCBI] 0.000230218
MMP20 [NCBI] 0.000142136
AMBN [NCBI] 0.000129754
DLX3 [NCBI] 8.20524e-05
FAM83H [NCBI] 1.42758e-05
KLK4 [NCBI] 1.07468e-05
GALNT3 [NCBI] 1.03488e-05
CKAP4 [NCBI] 5.28323e-06



OMIM


 OMIM Link Information
gain		 01
kohlschutter-tonz syndrome [NCBI] 0.00574248
cone-rod dystrophy and amelogenesis imperfecta [NCBI] 0.003153
amelogenesis imperfecta, hypoplastic type [NCBI] 0.003153
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 1 [NCBI] 0.00139904
AMELX [NCBI] 0.00121382
AIH2 [NCBI] 0.00113425
amelogenesis imperfecta, hypoplastic/hypomaturation, x-linked 2 [NCBI] 0.0010375
ENAM [NCBI] 0.000946354
trichodentoosseous syndrome [NCBI] 0.000692449
AIHHT [NCBI] 0.000581969
gonadal dysgenesis, xx type, with deafness [NCBI] 0.000545541
amelogenesis imperfecta, hypoplastic, and openbite malocclusion, autosomal recessive [NCBI] 0.000374235
amelogenesis imperfecta, pigmented hypomaturation type [NCBI] 0.000374235
AI1G [NCBI] 0.000374235
MMP20 [NCBI] 0.00025353
platyspondyly with amelogenesis imperfecta [NCBI] 0.000249088
hearing loss, sensorineural, with enamel hypoplasia and nail defects [NCBI] 0.000204157
KLK4 [NCBI] 0.000149701
amelogenesis imperfecta, local hypoplastic type, recessive [NCBI] 0.000124346
dentin dysplasia, type ii [NCBI] 7.55373e-05
AMBN [NCBI] 7.03962e-05
ODDD [NCBI] 5.05336e-05
GJA1 [NCBI] 2.36714e-05
TS [NCBI] 1.04043e-05



Database Center for Life Science